Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/121109
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dc.contributor.authorBarceló, Antonia-
dc.contributor.authorEsquinas López, Cristina-
dc.contributor.authorRobles, Juan-
dc.contributor.authorPiérola, Javier-
dc.contributor.authorPeña, Mónica de la-
dc.contributor.authorAguilar, Irene-
dc.contributor.authorMorell-Garcia, Daniel-
dc.contributor.authorAlonso, Alberto-
dc.contributor.authorToledo Pons, Nuria-
dc.contributor.authorSánchez de la Torre, Manuel-
dc.contributor.authorBarbé, Ferran-
dc.date.accessioned2018-03-26T12:10:14Z-
dc.date.available2018-03-26T12:10:14Z-
dc.date.issued2016-10-01-
dc.identifier.issn1389-9457-
dc.identifier.urihttp://hdl.handle.net/2445/121109-
dc.description.abstractBackground: obstructive sleep apnea (OSA) is now being recognized as an additional contributing factor to the pathogenesis of obesity-related comorbidities. At the same time, there is now increasing evidence to suggest that intestinal wall permeability plays a role in the development of metabolic syndrome. In the present study, circulating zonulin and fatty acid binding protein (I-FABP) were measured in association with metabolic, hepatic, and inflammatory parameters. Results: compared with controls, plasma I-FABP levels were significantly higher in patients with OSA (571 pg/mL [IQR 290-950] vs 396 pg/mL [IQR 234-559], p = 0.04). Zonulin levels were similar between groups. Significant relationships were observed between zonulin levels and waist circumference (p < 0.05), glucose (p < 0.05), and insulin (p < 0.05). In addition, in the OSA group, zonulin levels correlated negatively with the mean nocturnal oxygenation saturation (p < 0.05) and positively with total cholesterol (p < 0.05), alanine aminotransferase (ALT) (p < 0.005), aminotransferase (AST) (p < 0.01), gamma glutamyltransferase (GGT) (p < 0.005), and high-sensitivity C-reactive protein (hs-CRP) (p < 0.05). Multivariate analysis showed that associations between zonulin and ALT, AST, and hs-CRP were attenuated, but not eliminated, after adjustment for other variables. Conclusions: the results of this study suggest that OSA is a risk factor for intestinal damage, regardless of metabolic profile, and that intestinal permeability might be a possible contributor to nonalcoholic fatty liver disease in patients with OSA.-
dc.format.extent4 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.sleep.2016.01.019-
dc.relation.ispartofSleep Medicine, 2016, vol. 26, p. 12-15-
dc.relation.urihttps://doi.org/10.1016/j.sleep.2016.01.019-
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2016-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es-
dc.sourceArticles publicats en revistes (Infermeria de Salut Pública, Salut mental i Maternoinfantil)-
dc.subject.classificationProteïnes portadores-
dc.subject.classificationFixació de proteïnes-
dc.subject.classificationSíndrome metabòlica-
dc.subject.classificationAbsorció intestinal-
dc.subject.classificationSíndromes d'apnea del son-
dc.subject.classificationObesitat-
dc.subject.otherCarrier proteins-
dc.subject.otherProtein binding-
dc.subject.otherMetabolic syndrome-
dc.subject.otherIntestinal absorption-
dc.subject.otherSleep apnea syndromes-
dc.subject.otherObesity-
dc.titleGut epithelial barrier markers in patients with obstructive sleep apnea-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec678838-
dc.date.updated2018-03-26T12:10:14Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid28007354-
Appears in Collections:Articles publicats en revistes (Infermeria de Salut Pública, Salut mental i Maternoinfantil)

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